Suzanne Tamang
Stanford University · Rheumatology
Active 2004–2024
About
Suzanne Tamang is an Assistant Professor of Medicine specializing in Immunology and Rheumatology at Stanford University. She is affiliated with the Center for Artificial Intelligence in Medicine & Imaging (AIMI), where her work focuses on integrating artificial intelligence into healthcare, particularly in the fields of immunology and rheumatology. Her research involves leveraging AI technologies to improve diagnosis, treatment, and understanding of immune-related diseases, contributing to advancements in medical imaging and healthcare data analysis.
Research topics
- Machine Learning
- Computer Science
- Artificial Intelligence
- Medicine
- Medical emergency
- Psychology
- Biology
- Clinical psychology
- Psychiatry
- Intensive care medicine
Selected publications
PLoS ONE · 2022 · 35 citations
- Artificial Intelligence
- Machine Learning
- Computer Science
Mortality prediction for intensive care unit (ICU) patients is crucial for improving outcomes and efficient utilization of resources. Accessibility of electronic health records (EHR) has enabled data-driven predictive modeling using machine learning. However, very few studies rely solely on unstructured clinical notes from the EHR for mortality prediction. In this work, we propose a framework to predict short, mid, and long-term mortality in adult ICU patients using unstructured clinical notes from the MIMIC III database, natural language processing (NLP), and machine learning (ML) models. Depending on the statistical description of the patients' length of stay, we define the short-term as 48-hour and 4-day period, the mid-term as 7-day and 10-day period, and the long-term as 15-day and 30-day period after admission. We found that by only using clinical notes within the 24 hours of admission, our framework can achieve a high area under the receiver operating characteristics (AU-ROC) score for short, mid and long-term mortality prediction tasks. The test AU-ROC scores are 0.87, 0.83, 0.83, 0.82, 0.82, and 0.82 for 48-hour, 4-day, 7-day, 10-day, 15-day, and 30-day period mortality prediction, respectively. We also provide a comparative study among three types of feature extraction techniques from NLP: frequency-based technique, fixed embedding-based technique, and dynamic embedding-based technique. Lastly, we provide an interpretation of the NLP-based predictive models using feature-importance scores.
JAMA Psychiatry · 2022 · 55 citations
- Psychology
- Psychiatry
- Clinical psychology
Importance: Suicide is a leading cause of death; however, the molecular genetic basis of suicidal thoughts and behaviors (SITB) remains unknown. Objective: To identify novel, replicable genomic risk loci for SITB. Design, Setting, and Participants: This genome-wide association study included 633 778 US military veterans with and without SITB, as identified through electronic health records. GWAS was performed separately by ancestry, controlling for sex, age, and genetic substructure. Cross-ancestry risk loci were identified through meta-analysis. Study enrollment began in 2011 and is ongoing. Data were analyzed from November 2021 to August 2022. Main Outcome and Measures: SITB. Results: A total of 633 778 US military veterans were included in the analysis (57 152 [9%] female; 121 118 [19.1%] African ancestry, 8285 [1.3%] Asian ancestry, 452 767 [71.4%] European ancestry, and 51 608 [8.1%] Hispanic ancestry), including 121 211 individuals with SITB (19.1%). Meta-analysis identified more than 200 GWS (P < 5 × 10-8) cross-ancestry risk single-nucleotide variants for SITB concentrated in 7 regions on chromosomes 2, 6, 9, 11, 14, 16, and 18. Top single-nucleotide variants were largely intronic in nature; 5 were independently replicated in ISGC, including rs6557168 in ESR1, rs12808482 in DRD2, rs77641763 in EXD3, rs10671545 in DCC, and rs36006172 in TRAF3. Associations for FBXL19 and AC018880.2 were not replicated. Gene-based analyses implicated 24 additional GWS cross-ancestry risk genes, including FURIN, TSNARE1, and the NCAM1-TTC12-ANKK1-DRD2 gene cluster. Cross-ancestry enrichment analyses revealed significant enrichment for expression in brain and pituitary tissue, synapse and ubiquitination processes, amphetamine addiction, parathyroid hormone synthesis, axon guidance, and dopaminergic pathways. Seven other unique European ancestry-specific GWS loci were identified, 2 of which (POM121L2 and METTL15/LINC02758) were replicated. Two additional GWS ancestry-specific loci were identified within the African ancestry (PET112/GATB) and Hispanic ancestry (intergenic locus on chromosome 4) subsets, both of which were replicated. No GWS loci were identified within the Asian ancestry subset; however, significant enrichment was observed for axon guidance, cyclic adenosine monophosphate signaling, focal adhesion, glutamatergic synapse, and oxytocin signaling pathways across all ancestries. Within the European ancestry subset, genetic correlations (r > 0.75) were observed between the SITB phenotype and a suicide attempt-only phenotype, depression, and posttraumatic stress disorder. Additionally, polygenic risk score analyses revealed that the Million Veteran Program polygenic risk score had nominally significant main effects in 2 independent samples of veterans of European and African ancestry. Conclusions and Relevance: The findings of this analysis may advance understanding of the molecular genetic basis of SITB and provide evidence for ESR1, DRD2, TRAF3, and DCC as cross-ancestry candidate risk genes. More work is needed to replicate these findings and to determine if and how these genes might impact clinical care.
A Machine Learning Approach to Identifying Changes in Suicidal Language
Suicide and Life-Threatening Behavior · 2020 · 44 citations
- Machine Learning
- Artificial Intelligence
- Computer Science
OBJECTIVE: With early identification and intervention, many suicidal deaths are preventable. Tools that include machine learning methods have been able to identify suicidal language. This paper examines the persistence of this suicidal language up to 30 days after discharge from care. METHOD: In a multi-center study, 253 subjects were enrolled into either suicidal or control cohorts. Their responses to standardized instruments and interviews were analyzed using machine learning algorithms. Subjects were re-interviewed approximately 30 days later, and their language was compared to the original language to determine the presence of suicidal ideation. RESULTS: The results show that language characteristics used to classify suicidality at the initial encounter are still present in the speech 30 days later (AUC = 89% (95% CI: 85-95%), p < .0001) and that algorithms trained on the second interviews could also identify the subjects that produced the first interviews (AUC = 85% (95% CI: 81-90%), p < .0001). CONCLUSIONS: This approach explores the stability of suicidal language. When using advanced computational methods, the results show that a patient's language is similar 30 days after first captured, while responses to standard measures change. This can be useful when developing methods that identify the data-based phenotype of a subject.
Frequent coauthors
- 46 shared
David W. Oslin
University of Pennsylvania
- 45 shared
Nathan A. Kimbrel
Duke University
- 43 shared
Jean C. Beckham
Durham VA Health Care System
- 41 shared
Rafael Zamora‐Resendiz
Lawrence Berkeley National Laboratory
- 41 shared
Silvia Crivelli
Lawrence Berkeley National Laboratory
- 40 shared
Destinee Morrow
Lawrence Berkeley National Laboratory
- 39 shared
Esther L. Meerwijk
Center for Innovation
- 33 shared
Alex H. S. Harris
Stanford University
Education
Postdoctoral Scholar, Department of Biomedical Informatics
Stanford University
PhD, Computer Science
Graduate Center, City University of New York
Similar researchers at Stanford University
- Resume-aware match score
- Save to shortlist
- AI-drafted outreach
See your match with Suzanne Tamang
PhdFit ranks faculty by your research interests, methods, and publications — grounded in their actual work, not templates.
- Free to start
- No credit card
- 30-second signup